The following data is part of a premarket notification filed by Passy-muir, Inc. with the FDA for Passy-muir O2 Adapter; Pma2000.
| Device ID | K970365 |
| 510k Number | K970365 |
| Device Name: | PASSY-MUIR O2 ADAPTER; PMA2000 |
| Classification | Tube Tracheostomy And Tube Cuff |
| Applicant | PASSY-MUIR, INC. 4521 CAMPUS DR., SUITE 273 Irvine, CA 92612 |
| Contact | Patricia E Passy |
| Correspondent | Patricia E Passy PASSY-MUIR, INC. 4521 CAMPUS DR., SUITE 273 Irvine, CA 92612 |
| Product Code | JOH |
| CFR Regulation Number | 868.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-01-31 |
| Decision Date | 1997-02-12 |
| Summary: | summary |